J. Hata

Constitutional WT1 mutations correlate with clinical features in children with progressive nephropathy

A. Takata, R. Fukuzawa, S. Ito, 2000, Journal of medical genetics.

Do intronic mutations affecting splicing of WT1 exon 9 cause Frasier syndrome?

H. Yoneyama, Y. Akasaka, A. Takata, 1998, Journal of medical genetics.

A neuroblastoma cell line derived from a case detected through a mass screening system in Japan

M. Hamazaki, A. Takata, H. Hiraiwa, 1997, Cancer.

Wilms' tumor and the WT1 gene.

J. Hata, 1999, Contributions to nephrology.

Unusual Chromaffin Cell Differentiation of a Neuroblastoma After Chemotherapy and Radiotherapy: Report of an Autopsy Case With Immunohistochemical Evaluations

Y. Tsunematsu, K. Matsuoka, J. Hata, 2004, The American journal of surgical pathology.

Malignant fibrous histiocytoma of the cecum: Report of a case and review of the literature

N. Hiraoka, K. Maeda, Masako Suzuki, 1997, Pathology international.

Isolated diffuse mesangial sclerosis and Wilms tumor suppressor gene.

A. Takata, H. Hataya, S. Ito, 2001, The Journal of pediatrics.

Genomic changes in the WT-gene (WT1) in Wilms' tumors and their correlation with histology.

A. Umezawa, Y. Akasaka, H. Iri, 1992, The American journal of pathology.